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两名下丘脑错构瘤继发性早熟儿童肾上腺功能初现缺乏。

Lack of adrenarche in two children with precocious puberty secondary to hypothalamic hamartoma.

作者信息

Rappaport R, Brauner R

机构信息

Unit of Pediatric Endocrinology and Diabetes, Hôpital des Enfants Malades, Paris, France.

出版信息

Horm Res. 1989;31(5-6):226-9. doi: 10.1159/000181121.

Abstract

Adrenarche, which occurs earlier than gonadarche in normal children, is marked by increases in plasma dehydroepiandrosterone and its sulfate (DHAS). Adrenarche and gonadarche can be dissociated in various situations, e.g. central precocious puberty, indicating that they are controlled by independent mechanisms. This report concerns 2 children with central precocious puberty secondary to hypothalamic hamartoma. Their plasma basal DHAS values, compared to other cases with central precocious puberty not secondary to hamartoma, remained low for chronological age and bone age over a follow-up of 6.3 (case 1) and 9.2 9.2 years (case 2): in case 1 (boy), DHAS was 9 micrograms/dl at chronological age 7.7 and bone age 13 years; in case 2 (girl), DHAS was 11 micrograms/dl for chronological age 10.5 and bone age 13.5 years. GH secretion was normal. Basal plasma cortisol levels as the levels during hypoglycemia and after corticotropin stimulation were all normal. These data suggest that hypothalamic hamartoma may affect the central control of adrenarche. They may also contribute to the diagnosis of hypothalamic hamartoma.

摘要

在正常儿童中,肾上腺功能初现早于性腺功能初现,其特征是血浆脱氢表雄酮及其硫酸盐(DHAS)水平升高。肾上腺功能初现和性腺功能初现在多种情况下可分离,如中枢性性早熟,这表明它们受独立机制控制。本报告涉及2例继发于下丘脑错构瘤的中枢性性早熟儿童。与其他非继发于错构瘤的中枢性性早熟病例相比,在6.3年(病例1)和9.2年(病例2)的随访期间,他们的血浆基础DHAS值按实际年龄和骨龄计算仍较低:病例1(男孩),实际年龄7.7岁、骨龄13岁时,DHAS为9微克/分升;病例2(女孩),实际年龄10.5岁、骨龄13.5岁时,DHAS为11微克/分升。生长激素分泌正常。基础血浆皮质醇水平、低血糖期间及促肾上腺皮质激素刺激后的水平均正常。这些数据表明下丘脑错构瘤可能影响肾上腺功能初现的中枢控制。它们也可能有助于下丘脑错构瘤的诊断。

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